Clinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosis

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dc.contributor.authorŞişmanlar Eyüboğlu, Tuğba
dc.contributor.authorDoğru, Deniz
dc.contributor.authorÇakır, Erkan
dc.contributor.authorÇobanoğlu, Nazan
dc.contributor.authorPekcan, Sevgi
dc.contributor.authorCinel, Güzin
dc.contributor.authorYalçın, Ebru
dc.contributor.authorŞen, Velat
dc.contributor.authorŞen, Hadice Selimoğlu
dc.contributor.orcid0000-0001-7284-4999
dc.contributor.orcid0000-0001-9931-9473
dc.contributor.orcid0000-0002-1438-7854
dc.contributor.orcid0000-0002-3686-2927
dc.contributor.orcid0000-0002-9232-5982
dc.contributor.orcid0000-0002-2597-6646
dc.date.accessioned2024-04-24T15:59:31Z
dc.date.available2024-04-24T15:59:31Z
dc.date.issued2020
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Hastalıkları Ana Bilim Dalıen_US
dc.description.abstractBackground Pseudo-Bartter syndrome (PBS) is a rare complication of cystic fibrosis (CF) and there are limited data in the literature about it. We aimed to compare clinical features and accompanying findings of patients with PBS in a large patient population. Methods The data were collected from the Cystic Fibrosis Registry of Turkey where 1170 CF patients were recorded in 2017. Clinical features, diagnostic test results, colonization status, complications, and genetic test results were compared in patients with and without PBS. Results Totally 1170 patients were recorded into the registry in 2017 and 120 (10%) of them had PBS. The mean age of diagnosis and current age of patients were significantly younger and newborn screening positivity was lower in patients with PBS (P < .001). There were no differences between the groups in terms of colonization status, mean z-scores of weight, height, BMI, and mean FEV1 percentage. Types of genetic mutations did not differ between the two groups. Accompanying complications were more frequent in patients without PBS. Conclusion PBS was detected as the most common complication in the registry. It could be due to warm weather conditions of our country. It is usually seen in younger ages regardless of mutation phenotype and it could be a clue for early diagnosis of CF.en_US
dc.identifier.citationEyüboğlu, T. Ş., Doğru, D., Çakır, E., Çobanoğlu, N., Pekcan, S., Cinel, G. ve diğerleri. (2020). Clinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosis. Pediatric Pulmonology, 55(8), 2011-2016.
dc.identifier.doi10.1002/ppul.24805
dc.identifier.endpage2016en_US
dc.identifier.issn8755-6863
dc.identifier.issn1099-0496
dc.identifier.issue8en_US
dc.identifier.pmid32364312
dc.identifier.scopus2-s2.0-85085137196
dc.identifier.scopusqualityQ1
dc.identifier.startpage2011en_US
dc.identifier.urihttps://doi.org/10.1002/ppul.24805
dc.identifier.urihttps://hdl.handle.net/11468/14118
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/ppul.24805
dc.identifier.volume55en_US
dc.identifier.wosWOS:000530442700001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorŞen, Velat
dc.institutionauthorŞen, Hadice Selimoğlu
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofPediatric Pulmonology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCystic Fibrosisen_US
dc.subjectPseudo-Bartter Syndromeen_US
dc.subjectRegistryen_US
dc.titleClinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosisen_US
dc.titleClinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosis
dc.typeArticleen_US

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